Classifications

• • C—CHEMISTRY; METALLURGY
  • C07—ORGANIC CHEMISTRY
  • C07D—HETEROCYCLIC COMPOUNDS
  • C07D295/00—Heterocyclic compounds containing polymethylene-imine rings with at least five ring members, 3-azabicyclo [3.2.2] nonane, piperazine, morpholine or thiomorpholine rings, having only hydrogen atoms directly attached to the ring carbon atoms
  • C07D295/04—Heterocyclic compounds containing polymethylene-imine rings with at least five ring members, 3-azabicyclo [3.2.2] nonane, piperazine, morpholine or thiomorpholine rings, having only hydrogen atoms directly attached to the ring carbon atoms with substituted hydrocarbon radicals attached to ring nitrogen atoms
  • C07D295/08—Heterocyclic compounds containing polymethylene-imine rings with at least five ring members, 3-azabicyclo [3.2.2] nonane, piperazine, morpholine or thiomorpholine rings, having only hydrogen atoms directly attached to the ring carbon atoms with substituted hydrocarbon radicals attached to ring nitrogen atoms substituted by singly bound oxygen or sulfur atoms
  • C07D295/096—Heterocyclic compounds containing polymethylene-imine rings with at least five ring members, 3-azabicyclo [3.2.2] nonane, piperazine, morpholine or thiomorpholine rings, having only hydrogen atoms directly attached to the ring carbon atoms with substituted hydrocarbon radicals attached to ring nitrogen atoms substituted by singly bound oxygen or sulfur atoms with the ring nitrogen atoms and the oxygen or sulfur atoms separated by carbocyclic rings or by carbon chains interrupted by carbocyclic rings
• • A—HUMAN NECESSITIES
  • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
  • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
  • A61K31/00—Medicinal preparations containing organic active ingredients
  • A61K31/33—Heterocyclic compounds
  • A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
  • A61K31/495—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with two or more nitrogen atoms as the only ring heteroatoms, e.g. piperazine or tetrazines
• • C—CHEMISTRY; METALLURGY
  • C07—ORGANIC CHEMISTRY
  • C07D—HETEROCYCLIC COMPOUNDS
  • C07D295/00—Heterocyclic compounds containing polymethylene-imine rings with at least five ring members, 3-azabicyclo [3.2.2] nonane, piperazine, morpholine or thiomorpholine rings, having only hydrogen atoms directly attached to the ring carbon atoms
  • C07D295/04—Heterocyclic compounds containing polymethylene-imine rings with at least five ring members, 3-azabicyclo [3.2.2] nonane, piperazine, morpholine or thiomorpholine rings, having only hydrogen atoms directly attached to the ring carbon atoms with substituted hydrocarbon radicals attached to ring nitrogen atoms
  • C07D295/12—Heterocyclic compounds containing polymethylene-imine rings with at least five ring members, 3-azabicyclo [3.2.2] nonane, piperazine, morpholine or thiomorpholine rings, having only hydrogen atoms directly attached to the ring carbon atoms with substituted hydrocarbon radicals attached to ring nitrogen atoms substituted by singly or doubly bound nitrogen atoms
  • C07D295/135—Heterocyclic compounds containing polymethylene-imine rings with at least five ring members, 3-azabicyclo [3.2.2] nonane, piperazine, morpholine or thiomorpholine rings, having only hydrogen atoms directly attached to the ring carbon atoms with substituted hydrocarbon radicals attached to ring nitrogen atoms substituted by singly or doubly bound nitrogen atoms with the ring nitrogen atoms and the substituent nitrogen atoms separated by carbocyclic rings or by carbon chains interrupted by carbocyclic rings

Definitions

• An object of the present invention is the obtaining of a cyclobutane derivative selected from the group consisting of (1) a compound having the formula I ##SPC2##
• R 1 , R 2 and R 3 are members selected from the group consisting of hydrogen, halogen, hydroxy, trifluoromethyl, benzyloxy, alkyl having 1 to 6 carbon atoms, alkoxy having 1 to 3 carbon atoms, acyloxy where acyl is an acyl of an organic carboxylic acid having 1 to 12 carbon atoms, phenyl, cyclohexyl, and any two of R 1 , R 2 and R 3 taken together, methylenedioxy,
• R 4 is a member selected from the group consisting of hydrogen and alkyl having 1 to 2 carbon atoms,
• R 5 is a member selected from the group consisting of hydrogen and alkyl having 1 to 3 carbon atoms
• R 6 is a member selected from the group consisting of ##SPC3##
• R 7 and R 8 are members selected from the group consisting of hydrogen, halogen, trifluoromethyl, hydroxy, nitro, amino, benzyloxy, alkyl having 1 to 3 carbons, alkoxy having 1 to 3 carbon atoms, alkylthio having 1 to 3 carbon atoms and acyloxy where acyl is an acyl of an organic carboxylic acid having 1 to 12 carbon atoms, and
• R 9 is a member selected from the group consisting of hydrogen, halogen, hydroxy, nitro, amino, benzyloxy, carboxy, carbalkoxy having 1 to 3 carbon atoms in the alkoxy, alkyl having 1 to 3 carbon atoms, alkoxy having 1 to 3 carbon atoms and acyloxy where acyl is an acyl of an organic carboxylic acid having 1 to 12 carbon atoms,
• Another object of the present invention is the development of a process for the sedation and relaxing of muscles of warm-blooded animals comprising administering to warm-blooded animals a safe but effective amount of the above cyclobutane derivatives.
• a further object is to develop pharmaceutical compositions containing the above cyclobutane derivatives.
• the present invention relates to cyclobutane derivatives having the general formula I; as well as the process of obtaining the cyclobutane derivatives and the process of utilizing the same in pharmaceutical compositions for sedation and muscle relaxation.
• R 1 , R 2 and R 5 are hydrogen, R 3 is hydroxy, chloro or alkyl having 3 to 5 carbon atoms, R 4 is methyl and R 6 is phenyl, 4-hydroxyphenyl, 4-methoxyphenyl or pyridyl-2.
• R 1 , R 2 and R 5 are hydrogen
• R 3 is hydroxy, chloro or alkyl having 3 to 5 carbon atoms
• R 4 is methyl
• R 6 is phenyl, 4-hydroxyphenyl, 4-methoxyphenyl or pyridyl-2.
• R 3 ' is selected from the group consisting of hydroxy, chloro and alkyl having 3 to 5 carbon atoms and R 6 ' is selected from the group consisting of phenyl, 4-hydroxyphenyl, 4-methoxyphenyl and pyridyl-2, as well as the acid addition salts of said compounds with physiologically compatible inorganic or organic acids; where the 1-phenyl is in trans configuration to the cyclobutane ring with respect to the 3-piperazinyl.
• R 4 , R 5 and R 6 are defined as above, except that no radicals containing acyloxy and carbalkoxy groups are present, is reacted with a compound of general formula III, ##SPC6##
• R 1 ' to R 3 ' represent hydrogen atoms, halogen atoms, hydroxyl groups protected by a protective group, trifluoromethyl groups, alkyl groups with 1 to 6 carbon atoms, alkoxy groups with 1 to 3 carbon atoms or 2 of the radicals R 1 ' to R 3 ' together represents a methylenedioxy group and M represents an alkali metal such as lithium or a magnesium halogenide group.
• the reaction is preferably carried out in an anhydrous inert solvent such as ether, tetrahydrofuran or ethylene glycoldimethylether, optionally under a protective gas atmosphere and appropriately at temperatures between -20°C and 100°C, preferably however at the boiling temperature of the solvent used.
• an optionally used protective group for a hydroxy group in a compound of general formula III is split off, for example the benzyl group by means of catalytical hydrogenation or the trimethylsilyl group by means of hydrolysis.
• R 6 is defined as above, and Hal represents a chlorine, bromine or iodine atom.
• the reaction is appropriately carried out in a solvent such as ethanol, water/ethanol, isopropanol, butanol, dioxane or xylene, optionally in the presence of potassium iodide or in the presence of a catalyst, for example copper powder or anhydrous zinc chloride, and optionally in the presence of an inorganic or organic base, for example an alkali metal carbonate such as sodium carbonate, potassium carbonate or triethylamine, and according to the reactivity of the halogenide used at temperatures between 20°C and 160°C, preferably, however, at 80°C to 130°C.
• a solvent such as ethanol, water/ethanol, isopropanol, butanol, dioxane or xylene
• a catalyst for example copper powder or anhydrous zinc chloride
• an inorganic or organic base for example an alkali metal carbonate such as sodium carbonate, potassium carbonate or triethylamine
• the reactivity of the halogen atom in a compound of general formula V may be enhanced, if necessary, by the introduction of activating groups, e.g. one or more nitro groups and optionally in addition by the conversion, where R 6 is a pyridyl, of the pyridine-nitrogen into the N-oxide, e.g. by means of hydrogen peroxide or a peracid such as perbenzoic acid.
• activating groups e.g. one or more nitro groups and optionally in addition by the conversion, where R 6 is a pyridyl, of the pyridine-nitrogen into the N-oxide, e.g. by means of hydrogen peroxide or a peracid such as perbenzoic acid.
• the compound obtained is converted by means of reduction, e.g. by means of nascent or catalytically activated hydrogen, into the corresponding compound, optionally substituted by one or more amino groups, which on its part may be converted into the desired compound of general formula I
• protective groups e.g. by benzyl or trimethylsilyl groups.
• These protective groups may be split off again after the reaction, e.g. the benzyl group by means of catalytical hydrogenation and the trimethylsilyl group by means of hydrolysis.
• R 1 , R 2 , R 3 and R 4 are defined as above and X represents a halogen atom or the p-toluenesulfonyloxy group, is reacted with an amine of general formula VII,
• R 6 is defined as above.
• reaction is optionally carried out in a solvent such as propanol, dioxane or in an excess of the amine used of general formula VII and optionally in the presence of a base such as sodium carbonate, appropriately at temperatures between 50°C and 200°C, preferably however at the boiling temperature of the solvent used.
• a solvent such as propanol, dioxane or in an excess of the amine used of general formula VII and optionally in the presence of a base such as sodium carbonate, appropriately at temperatures between 50°C and 200°C, preferably however at the boiling temperature of the solvent used.
• a compound of general formula I is obtained, which is substituted by one or more halogen atoms
• this compound may be dehalogenated by means of usual dehalogenating agents, e.g. by means of catalytical hydrogenation in the presence of palladium-coal and sodium acetate, or if a cis-trans mixture of a compound of general formula I is obtained, this mixture may be separated into the corresponding cis and trans compounds, for example by means of column chromatography and/or if a compound of general formula I is obtained, wherein the radicals R 1 to R 3 represent acyloxy groups and/or R 6 contains an acyloxy and/or carbalkoxy group, these groups may, for example be converted into the free hydroxy groups or respectively the carboxyl group by means of hydrolysis, and/or if a compound of general formula I is obtained, which contains free hydroxy groups, this compound may subsequently be acylated, if desired, with an acylating agent such as
• the acylating agent and the acyloxy group are derived from acyls of organic carboxylic acids having 1 to 12 carbon atoms, more particularly alkanoic acids such as acetic acid, isobutyric acid, etc.; and aromatic hydrocarbon carboxylic acids such as benzoic acid. etc.
• the obtained compounds of general formula I may be converted into their salts with the corresponding physiologically compatible inorganic or organic acids or, where R 9 is carboxyl, bases.
• acids for example, inorganic acids such as hydrochloric acid, hydrobromic acid, sulfuric acid and phosphoric acid, and organic acids having 1 to 6 carbon atoms, preferably those containing at least one hydroxyl, such as lactic acid, citric acid, tartaric acid and maleic acid and as bases alkali metal hydroxides, carbonates and ammonium hydroxide, such as sodium hydroxide and potassium hydroxide have proved to be suitable.
• a compound of general formula II used as starting material may be prepared by cycloaddition of an enamine of general formula VIII, ##SPC9##
• R 5 and R 6 are defined as above, with a ketene of general formula IX, ##EQU1## wherein R 4 is defined as above, in a solvent such as benzene and at temperatures between 20°C and 80°C and by subsequent hydrolysis of an optionally obtained O-acylated compound (see Angew. Chemie 74, 32 (1962); J. Org. Chem. 26, 4775 (1961) and ibid 26, 4776 (1961)).
• a compound of general formula VI used as starting material is obtained by addition of ethyleneoxide to an amine of general formula X, ##SPC10##
• R 1 to R 4 are defined as above, and subsequent reaction with a halogenating agent such as thionyl chloride.
• An amine of general formula X is obtained from the corresponding dibenzyl-compound by hydrogenating removal of the benzyl groups in the presence of palladium/coal.
• the necessary dibenzyl-compound is obtained by Grignard reaction of a corresponding cyclobutanone-derivate, which may be prepared by cycloaddition from the corresponding enamine with the corresponding ketene.
• a compound of general formula IV used as starting material is obtained by reaction of a corresponding substituted cyclobutanone with a corresponding Grignard compound and subsequent removal of the protective group in 4-position of the piperazine, e.g. the benzyl group, in the obtained cyclobutanol-compound for example by means of catalytical hydrogenation.
• trans is utilized in reference to the position of the piperazine ring in comparison to the aromatic nucleus which is in 1-position of the cyclobutane ring.
• Example 72 Prepared analogously to Example 72 by hydrogenation of 1-(4-benzyloxyphenyl)-2,2,4,4-tetramethyl-3-[4-phenyl-piperazinyl]-cyclobutanol-(1) in ethanol over palladium on carbon at room temperature. Purification by means of column chromatography. Yield: 57% of theory; m.p. 198°-200°C (from benzene).
• Example 72 Prepared analogously to Example 72 by hydrogenation of 1-(3-benzyloxyphenyl)-2,2,4,4-tetramethyl-3-[4-phenyl-piperazinyl]-cyclobutanol-(1) in ethanol over palladium on carbon at 50°C. Purification by means of column chromatography. Yield: 39% of theory; m.p. 210°-211°C (from methanol).
• Example 78 Prepared analogously to Example 78 by reaction of 1-(4-hydroxyphenyl)-2,2,4,4-tetramethyl-3-[4-(pyridyl-2)-piperazinyl]-cyclobutanol-(1) with benzoylchloride in the presence of potassium carbonate in boiling dioxane. Yield: 51% of theory; m.p. 180°-182°C (from ethyl acetate).
• Example 78 Prepared analogously to Example 78 by reaction of 1-(4-hydroxyphenyl)-2,2,4,4-tetramethyl-3-[4-(pyridyl-2)-piperazinyl]-cyclobutanol-(1) with isobutyrylchloride in the presence of potassium carbonate in boiling acetone. Yield: 54% of theory; m.p. 133°-135°C (from acetone).
• Example 78 Prepared analogously to Example 78 by reaction of 1-phenyl-2,2,4,4-tetramethyl-3-[4-(4-hydroxyphenyl)-piperazinyl]-cyclobutanol-(1) with benzoylchloride in the presence of potassium carbonate in boiling dioxane. Yield: 8% of theory; m.p. 197°-198°C (from methanol).
• Example 78 Prepared analogously to Example 78 by reaction of 1-phenyl-2,2,4,4-tetramethyl-3-[4-(4-hydroxyphenyl)-piperazinyl]-cyclobutanol-(1) with isobutyrylchloride in the presence of triethylamine in ether at 20°C. Yield: 47% of theory; m.p. 148°-149°C (from petroleum ether).
• Example 76 Prepared analogously to Example 76 by acetylation of 1-phenyl-2,2,4,4-tetramethyl-3-[4-(3-hydroxy-pyridyl-2)-piperazinyl]-cyclobutanol-(1) with acetic acid anhydride in pyridine. Yield: 47% of theory; m.p. 165°-166°C (from ethanol).
• Example 72 Prepared analogously to Example 72 by hydrogenation of 1-phenyl-2,2,4,4-tetramethyl-3-[4-(3-benzyloxy-pyridyl-2)-piperazinyl]-cyclobutanol-(1) in methanol/water (9:1) over palladium on carbon at room temperature. Purification by means of column chromatography. Yield: 43% of theory; m.p. 196°-197°C.
• Example 72 Prepared analogously to Example 72 by hydrogenation of 1-(4-hydroxyphenyl)-2,2,4,4-tetramethyl-3-[4-(3-benzyloxy-pyridyl-2)-piperazinyl]-cyclobutanol-(1) in methanol/water (9:1) over palladium on carbon at room temperature. Purification by means of column chromatography. Yield: 43% of theory; m.p. 218°-220°C.
• the aqueous phase was made alkaline with diluted sodium hydroxide solution and extracted with ether (three times). After evaporation the crude product was dissolved in ethyl acetate and converted into its dihydrochloride by addition of etheric hydrochloric acid. When filtered off 1.2 gm (65% of theory) of crystals of the dihydrochloride were obtained. M.p. 238°C (decmop.).
• Example 96 Prepared analogously to Example 96 by reaction of 1-phenyl-2,2,4,4-tetramethyl-3-piperazinyl-cyclobutanol-(1) with 2-bromopyridine-3-carboxylic acid methyl ester in the presence of potassium carbonate in xylene at 100°C. Yield: 18% of theory; m.p. 181°-182°C (from methanol).
• Example 96 Prepared analogously to Example 96 by reaction of 1-(4-hydroxyphenyl)-2,2,4,4-tetramethyl-3-piperazinyl-cyclobutanol-(1) (m.p. of the crude product: 208°-209°C, decomp.) with 2-bromopyridine-3-carboxylic acid ethyl ester in the presence of triethylamine in boiling ethanol (99%). Isolation by means of column chromatography over silica gel. Yield: 25% of theory; m.p. 162°-163°C (from ether/petroleum ether).
• Example 96 Prepared analogously to Example 96 by reaction of 1-phenyl-2,2,4,4-tetramethyl-3-piperazinyl-cyclobutanol-(1) with 2-iodopyridine in the presence of water-free zinc-chloride in xylene at 130°C. Purified by means of column chromatography over silica gel. Yield: 12% of theory; m.p. 134°-136°C.
• the cyclobutane compounds of the general formula I are employed in pharmaceutical compositions customary in the field of sedation and muscle relaxation.
• the compositions contain a minor amount of the active cyclobutane compounds of the general formula I and a major amount of a pharmaceutical carrier.
• the pharmaceutical compositions may be in the form of injectable solutions or suspensions, tablets, coated tablets, dragees, sustained release tablets, suppositories, etc.
• the usual dose is 0.1 to 100 mgm, preferably 0.5 to 5 mgm, and more particularly 1 to 2 mgm, whether administered orally, parentally, or rectally.
• Substances I-III were mixed and moistened evenly with an aqueous solution of substance IV. Granulation: moist 1.5 mm; dry 1.0 mm. Substance V was mixed with the mass which was then pressed to tablets. Diameter: 7 mm, punch: flat with facet.
• Substances I-III were mixed and moistened evenly with an aqueous solution of IV.
• Granulation moist 1 mm, dry 0.75 mm, drying at 50°C.
• Substance V was mixed with the granulate which was then pressed into tablets with a diameter of 5 mm, Radius of convexity: 3.75 mm.
• Coating According to the usual sugar coating. Weight of coated tablet: 80 mgm.
• the suppository mass was molten. At 38°C the granulated active ingredient was dispersed homogeneously in the molten mass which was then cooled to 35°C and poured into pre-cooled suppository moulds. Weight of suppository: 1.7 gm.
• the active ingredient and the sorbitol were dissolved in distilled water. The mixture was made up to the indicated volume and filtered sterile. Filling: into brown 1 ml ampules. Sterilization: 20 minutes at 120°C.
• the new compounds of general formula I possess valuable pharmacological properties, especially a central depressant, sedative, muscle relaxing and anxiolytic activity.
• Another aspect of the invention is the method of sedation and relaxing of muscles in warm-blooded animals comprising administering to warm-blooded animals a safe but effective amount of at least one of the compounds of general formula I, alone or in a pharmaceutical composition.
• the said compounds may be administered orally, parentally or rectally.
• the usual dosage is from 0.002 to 5 mgm/kg, depending on the method of administration.
• F trans-1-(4-isopropylphenyl)-2,2,4,4-tetramethyl-3-(4-phenyl-piperazinyl)-cyclobutanol-(1),
• N trans-1-(4-isobutylphenyl)-2,2,4,4-tetramethyl-3-(4-phenyl-piperazinyl)-cyclobutanol-(1),
• R trans-1-(3-chlorophenyl)-2,2,4,4-tetramethyl-3-[4-(pyridyl-2)-piperazinyl]-cyclobutanol-(1).
• mice 1. muscle relaxing and sedative activity in mice:
• the muscle relaxing and sedative activity was tested according to the method of Young and Lewis (Science 105, 368 (1947)) with female NMRI-mice of a specific breed having a body weight of from 20 to 26 gm.
• the test apparatus comprises slowly turning wire cylinders, sloped for 30° against the vertical line (length: 43 cm; diameter: 22 cm; mesh-size of the wire netting: 0.6 cm).
• ED 50 The dose which caused 50% of the animals to fall out after certain test times was determined graphically:
• the acute toxicity was determined after oral administration to groups of 10 mice (sex ratio 1:1) from our own breeding colony.
• the LD 50 was measured by graphical extrapolation according to the method of Litchfield and Wilcoxon (J. Pharmacol. Exp. Therap. 96, 99 (1949) from the percentage of the animals which died within a period of 14 days after application of various doses:

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• 1973
  • 1973-10-25 NL NL7314672A patent/NL7314672A/xx not_active Application Discontinuation
  • 1973-11-06 US US05/413,233 patent/US3931185A/en not_active Expired - Lifetime
  • 1973-11-06 SU SU1967687A patent/SU524516A3/ru active
  • 1973-11-07 CH CH1563373A patent/CH587253A5/xx not_active IP Right Cessation
  • 1973-11-07 CH CH1470976A patent/CH602669A5/xx not_active IP Right Cessation
  • 1973-11-07 PH PH15192A patent/PH10668A/en unknown
  • 1973-11-08 BG BG024952A patent/BG23007A3/xx unknown
  • 1973-11-09 DD DD174561A patent/DD110271A5/xx unknown
  • 1973-11-09 GB GB5219273A patent/GB1410303A/en not_active Expired
  • 1973-11-09 CA CA185,407A patent/CA999297A/en not_active Expired
  • 1973-11-09 JP JP48126150A patent/JPS49133383A/ja active Pending
  • 1973-11-09 HU HUTO941A patent/HU167390B/hu unknown
  • 1973-11-09 AT AT943373A patent/AT334903B/de not_active IP Right Cessation
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  • 1973-11-09 FR FR7339898A patent/FR2206094B1/fr not_active Expired
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• 1974
  • 1974-06-22 ES ES427559A patent/ES427559A1/es not_active Expired
  • 1974-10-23 SU SU2069584A patent/SU561513A3/ru active

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